K-number	K061231
Device name	WELLFLEX BILIARY RX STENT SYSTEM
Applicant	Boston Scientific Corp
Product code	FGE
Device class	Class II
Decision date	Sep 1, 2006
Decision	Unknown
Regulation	876.5010

AI Summary

AI extraction for this record is queued and will appear within 24 hours. View full FDA record →

Source

View the full FDA submission: accessdata.fda.gov

Researching this as a predicate?

Want a transparent AI-ranking score, AI-discovered related predicates, ongoing safety and warning-letter monitoring, full predicate chain lineage, and a drafted SE rationale — all saved to your own project? That's what an account adds.

Start free trial →

Building an AI or ML-enabled device? Predicate search, PCCP tracking, and AI-specific FDA intelligence — built exclusively for AI/ML devices. Try AIFDA Intel →

WELLFLEX BILIARY RX STENT SYSTEM

Everything you need for a 510(k) submission. Nothing you don't.